Aldicarb

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Identification

Molecular formula
C7H14N2O2S
CAS Number
116-06-3
IUPAC Name
(2,2-dimethylchroman-8-yl) N-methylcarbamate
Molecular Weight
190.24g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.1800g/cm3
Synonyms
Niagara 11637
Interesting facts

Interesting Facts about (2,2-dimethylchroman-8-yl) N-methylcarbamate

(2,2-dimethylchroman-8-yl) N-methylcarbamate is a fascinating compound that merges the worlds of organic chemistry and medicinal applications. This compound is in the class of carbamates, which are known for their diverse biological activities.

Key Highlights

  • Biological Relevance: Carbamates exhibit a wide range of pharmacological effects, making them crucial in drug development. They can act as enzyme inhibitors and have applications in treating various diseases.
  • Structure and Function: The unique chroman ring structure contributes to the compound's properties. The dimethyl substitution on the chroman enhances its lipophilicity, potentially impacting the bioavailability and interaction with biological targets.
  • Synthesis: The synthesis of this compound typically involves multistep organic reactions that may include nucleophilic substitutions and coupling reactions, showcasing the versatility of organic synthesis techniques.
  • Environmental Impact: As with many carbamates, the potential for environmental persistence and toxicity is an aspect that researchers continuously study, leading to the development of safer alternatives.

Research into compounds like (2,2-dimethylchroman-8-yl) N-methylcarbamate opens avenues for new therapeutic agents and enhances our understanding of complex organic molecules. As the field of medicinal chemistry evolves, this compound exemplifies the synergy of chemistry and pharmacology, making it an exciting topic for further investigation.

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